EP0754704B1

EP0754704B1 - Synthetic antigens for the detection of antibodies to hepatitis C virus

Info

Publication number: EP0754704B1
Application number: EP96201157A
Authority: EP
Inventors: Robert J. Deleys; Dirk Pollet; Geert Maertens; Hugo Van Heuverswyn
Original assignee: Innogenetics NV SA
Current assignee: Fujirebio Europe NV SA
Priority date: 1990-12-14
Filing date: 1990-12-14
Publication date: 1999-10-06
Anticipated expiration: 2010-12-14
Also published as: WO1992010514A3; ES2138784T3; DK0489968T3; IL100158A; DK0644202T3; EP0489968A1; GR3032150T3; KR0181344B1; CY2043A; HU9202645D0; AU652013B2; SG47062A1; ATE144993T1; HU218357B; DE69030124T2; EP0644202A1; EP0644202B1; ATE185350T1; ATE149522T1; US5922532A

Abstract

Peptide sequences are provided which are capable of mimicking proteins encoded by HCV for use as reagents for screening of blood and blood products for prior exposure to HCV. The peptides are at least 5 amino acids long and can be used in various specific assays for the detection of antibodies to HCV, for the detection of HCV antigens, or as immunogens.

Description

The implementation of systematic testing for hepatitis B virus (HBV) has been instrumental in eliminating this virus from the blood supply. Nevertheless, a significant number of post-transfusion hepatitis (PTH) cases still occur. These cases are generally attributable to non-A, non-B hepatitis (NANBH) virus(es), the diagnosis of which is usually made by exclusion of other viral markers.
The etiological agent responsible for a large proportion of these cases has recently been cloned (Choo, Q-L et al. Science (1988) 244:359-362) and a first-generation antibody test developed (Kuo, G. et al. Science (1989) 244:362-364). The agent has been identified as a positive-stranded RNA virus, and the sequence of its genome has been partially determined. Studies suggest that this virus, referred to subsequently as hepatitis C virus (HCV), may be related to flaviviruses and pestiviruses. A portion of the genome of an HCV isolated from a chimpanzee (HCV_CDC/CHI) is disclosed in EP 0318216. The coding sequences disclosed in this document do not include sequences originating from the 5'-end of the viral genome which code for putative structural proteins. Recently however, sequences derived from this region of the HCV genome have been published (Okamoto, H. et al., Japan J. Exp. Med. 60:167-177, 1990.). The amino acid sequences encoded by the Japanese clone HC-J1 were combined with the HCV_CDC/CHI sequences in a region where the two sequences overlap to generate the composite sequence depicted in Figure 1. Specifically, the two sequences were joined at glycine₄₅₁. It should be emphasized that the numbering system used for the HCV amino acid sequence is not intended to be absolute since the existence of variant HCV strains harboring deletions or insertions is highly probable. Sequences corresponding to the 5' end of the HCV genome have also recently been disclosed in EP 0388232.
In order to detect potential carriers of HCV, it is necessary to have access to large amounts of viral proteins. In the case of HCV, there is currently no known method for culturing the virus, which precludes the use of virus-infected cultures as a source of viral antigens. The current first-generation antibody test makes use of a fusion protein containing a sequence of 363 amino acids encoded by the HCV genome. It was found that antibodies to this protein could be detected in 75 to 85% of chronic NANBH patients. In contrast, only approximately 15% of those patients who were in the acute phase of the disease, had antibodies which recognized this fusion protein (Kuo, G. et al. Science (1989) 244:362-364). The absence of suitable confirmatory tests, however, makes it difficult to verify these statistics. The seeming similarity between the HCV genome and that of flaviviruses makes it possible to predict the location of epitopes which are likely to be of diagnostic value. An analysis of the HCV genome reveals the presence of a continuous long open reading frame. Viral RNA is presumably translated into a long polyprotein which is subsequently cleaved by cellular and/or viral proteases. By analogy with, for example, Dengue virus, the viral structural proteins are presumed to be derived from the amino-terminal third of the viral polyprotein. At the present time, the precise sites at which the polyprotein is cleaved can only be surmised. Nevertheless, the structural proteins are likely to contain epitopes which would be useful for diagnostic purposes, both for the detection of antibodies as well as for raising antibodies which could subsequently be used for the detection of viral antigens. Similarly, domains of nonstructural proteins are also expected to contain epitopes of diagnostic value, even though these proteins are not found as structural components of virus particles.

Brief Description of the Drawings

Figure 1: shows the amino acid sequence of the composite HCV_{HC-J1/CDC/CHI}
Figure 2: shows the antibody binding to individual peptides and various mixtures in an ELISA assay

Description of the Specific Embodiments

It is known that RNA viruses frequently exhibit a high rate of spontaneous mutation and, as such, it is to be expected that no two HCV isolates will be completely identical, even when derived from the same individual. For the purpose of this disclosure, a virus is considered to be the same or equivalent to HCV if it exhibits a global homology of 60 percent or more with the HCV_{HC-J1/CDC/CHI} composite sequence at the nucleic acid level and 70 percent at the amino acid level.
The present invention relates more particularly to a peptide composition comprising at least one peptide selected from:
Additional amino acids or chemical groups may be added to the amino- or carboxyl terminus for the purpose of creating a "linker arm" by which the peptide can conveniently be attached to a carrier. The linker arm will be at least one amino acid and may be as many as 60 amino acids but will most frequently be 1 to 10 amino acids. The nature of the attachment to a solid phase or carrier need not be covalent.
Natural amino acids such as cysteine, lysine, tyrosine, glutamic acid, or aspartic acid may be added to either the amino- or carboxyl terminus to provide functional groups for coupling to a solid phase or a carrier. However, other chemical groups such as, for example, biotin and thioglycolic acid, may be added to the termini which will endow the peptides with desired chemical or physical properties. The termini of the peptides may also be modified, for example, by N-terminal acetylation or terminal carboxy-amidation. The peptides of interest are described in relation to the composite amino acid sequence shown in Figure 1. The amino acid sequences are given in the conventional and universally accepted three-letter code. In addition to the amino acids shown, other groups are defined as follows: Y is, for example, NH₂, one or more N-terminal amino acids, or other moieties added to facilitate coupling. Y may itself be modified by, for example, acetylation. Z is a bond, (an) amino acid(s), or (a) chemical group(s) which may be used for linking. X is intended to represent OH, NH₂, or a linkage involving either of these two groups.
Of particular interest is the use of the mercapto-group of cysteines or thioglycolic acids used for acylating terminal amino groups for cyclizing the peptides or coupling two peptides together. The cyclization or coupling may occur via a single bond or may be accomplished using thiol-specific reagents to form a molecular bridge.
The peptides may be coupled to a soluble carrier for the purpose of either raising antibodies or facilitating the adsorption of the peptides to a solid phase. The nature of the carrier should be such that it has a molecular weight greater than 5000 and should not be recognized by antibodies in human serum. Generally, the carrier will be a protein. Proteins which are frequently used as carriers are keyhole limpet hemocyanin, bovine gamma globulin, bovine serum albumin, and poly-L-lysine.
There are many well described techniques for coupling peptides to carriers. The linkage may occur at the N-terminus, C-terminus or at an internal site in the peptide. The peptide may also be derivatized for coupling. Detailed descriptions of a wide variety of coupling procedures are given, for example, in Van Regenmortel, M.H.V., Briand, J.P., Muller, S., and Plaué, S., Laboratory Techniques in Biochemistry and Molecular Biology, Vol. 19, Synthetic Polypeptides as Antigens, Elsevier Press, Amsterdam, New York, Oxford, 1988.
The peptides may also be synthesized directly on an oligo-lysine core in which both the alpha as well as the epsilon-amino groups of lysines are used as growth points for the peptides. The number of lysines comprising the core is preferably 3 or 7. Additionally, a cysteine may be included near or at the C-terminus of the complex to facilitate the formation of homo- or heterodimers. The use of this technique has been amply illustrated for hepatitis B antigens (Tam, J.P., and Lu, Y-A., Proc. Natl. Acad. Sci. USA (1989) 86:9084-9088) as well as for a variety of other antigens (see Tam, J.P., Multiple Antigen Peptide System: A Novel Design for Synthetic Peptide Vaccine and Immunoassay, in Synthetic Peptides, Approaches to Biological Problems, Tam, J.P., and Kaiser, E.T., ed. Alan R. Liss Inc., New York, 1989).
Depending on their intended use, the peptides may be either labeled or unlabeled. Labels which may be employed may be of any type, such as enzymatic, chemical, fluorescent, luminescent, or radioactive. In addition, the peptides may be modified for binding to surfaces or solid phases, such as, for example, microtiter plates, nylon membranes, glass or plastic beads, and chromatographic supports such as cellulose, silica, or agarose. The methods by which peptides can be attached or bound to solid support or surface are well known to those versed in the art.
Antibodies which recognize the peptides can be detected in a variety of ways. A preferred method of detection is the enzyme-linked immunosorbant assay (ELISA) in which a peptide or mixture of peptides is bound to a solid support. In most cases, this will be a microtiter plate but may in principle be any sort of insoluble solid phase. A suitable dilution or dilutions of serum or other body fluid to be tested is brought into contact with the solid phase to which the peptide is bound. The incubation is carried out for a time necessary to allow the binding reaction to occur. Subsequently, unbound components are removed by washing the solid phase. The detection of immune complexes is achieved using antibodies which specifically bind to human immunoglobulins, and which have been labeled with an enzyme, preferably but not limited to either horseradish peroxidase, alkaline phosphatase, or beta-galactosidase, which is capable of converting a colorless or nearly colorless substrate or co-substrate into a highly colored product or a product capable of forming a colored complex with a chromogen. Alternatively, the detection system may employ an enzyme which, in the presence of the proper substrate(s), emits light. The amount of product formed is detected either visually, spectrophotometrically, electrochemically, or luminometrically, and is compared to a similarly treated control. The detection system may also employ radioactively labeled antibodies, in which case the amount of immune complex is quantified by scintillation counting or gamma counting.
Other detection systems which may be used include those based on the use of protein A derived from Staphylococcus aureus Cowan strain I, protein G from group C Staphylococcus sp. (strain 26RP66), or systems which make use of the high affinity biotin-avidin or streptavidin binding reaction.
Antibodies raised to carrier-bound peptides can also be used in conjunction with labeled peptides for the detection of antibodies present in serum or other body fluids by competition assay. In this case, antibodies raised to carrier-bound peptides are attached to a solid support which may be, for example, a plastic bead or a plastic tube. Labeled peptide is then mixed with suitable dilutions of the fluid to be tested and this mixture is subsequently brought into contact with the antibody bound to the solid support. After a suitable incubation period, the solid support is washed and the amount of labeled peptide is quantified. A reduction in the amount of label bound to the solid support is indicative of the presence of antibodies in the original sample. By the same token, the peptide may also be bound to the solid support. Labeled antibody may then be allowed to compete with antibody present in the sample under conditions in which the amount of peptide is limiting. As in the previous example, a reduction in the measured signal is indicative of the presence of antibodies in the sample tested.
Another preferred method of antibody detection is the homogeneous immunoassay. There are many possible variations in the design of such assays. By way of example, numerous possible configurations for homogeneous enzyme immunoassays and methods by which they may be performed are given in Tijssen, P., Practice and Theory of Enzyme Immunoassays, Elsevier Press, Amersham, Oxford, New York, 1985. Detection systems which may be employed include those based on enzyme channeling, bioluminescence, allosteric activation and allosteric inhibition. Methods employing liposome-entrapped enzymes or coenzymes may also be used (see Pinnaduwage, P. and Huang, L., Clin. Chem. (1988) 34/2: 268-272, and Ullman, E.F. et al., Clin. Chem. (1987) 33/9: 1579-1584 for examples).
The synthesis of the peptides can be achieved in solution or on a solid support. Synthesis protocols generally employ the use t-butyloxycarbonyl- or 9-fluorenylmethoxy-carbonyl-protected activated amino acids. The procedures for carrying out the syntheses, the types of side-chain protection, and the cleavage methods are amply described in, for example, Stewart and Young, Solid Phase Peptide Synthesis, 2nd Edition, Pierce Chemical Company, 1984; and Atherton and Sheppard, Solid Phase Peptide Synthesis, IRL Press, 1989.

Experimental

I. Peptide Synthesis All of the peptides described were synthesized on Pepsyn K polyamide-Kieselguhr resin (Milligen, Novato, California) which had been functionalized with ethylenediamine and onto which the acid-labile linker 4-(alpha-Fmoc-amino-2',4'-dimethoxybenzyl) phenoxyacetic acid had been coupled (Rink, Tetrahedron Lett. (1987) 28:3787). t-Butyl-based side-chain protection and Fmoc alpha-amino-protection was used. The guanidino-group of arginine was protected by the 2,2,5,7,8-pentamethylchroman-6-sulfonyl moiety. The imidazole group of histidine was protected by either t-Boc or trityl and the sulfhydryl group of cysteine was protected by a trityl group. Couplings were carried out using performed O-pentafluorophenyl esters except in the case of arginine where diisopropylcarbodiimide-mediated hydroxybenzotriazole ester formation was employed. Except for peptide I, all peptides were N-acetylated using acetic anhydride. All syntheses were carried out on a Milligen 9050 PepSynthesizer (Novato, California) using continuous flow procedures.
Following cleavage with trifluoroacetic acid in the presence of scavengers and extraction with diethylether, all peptides were analyzed by C₁₈ -reverse phase chromatography.
Peptide I corresponds to amino acids 1 to 20 and has the following amino acid sequences:
Peptide II corresponds to amino acids 7 to 26 and has the amino acid sequence:
Peptide IIA corresponds to:
Peptide III corresponds to amino acids 13 to 32 and has the sequence:
Peptide IV corresponds to amino acid 37 to 56 and has the sequences:
Peptide V corresponds to amino acids 49 to 68 and has the sequence:
Peptide VI corresponds to amino acid 61 to 80 and has the following sequence:
Peptide VII corresponds to amino acids 73 to 92 and has the sequence:
Peptide XVI corresponds to amino acids 2275 to 2294 and has the sequence:
Peptide XVII corresponds to amino acids 2287 to 2306 and has the sequence:
Peptide XVIII corresponds to amino acids 2299 to 2318 and has the sequence:
Peptide XIX corresponds to amino acids 2311 to 2330 and has the sequence:

II. Detection of Antibodies to Hepatitis C Virus

A. Use of peptides bound to a nylon membrane. Peptides were dissolved in a suitable buffer to make a concentrated stock solution which was then further diluted in phosphate-buffered saline (PBS) or sodium carbonate buffer, pH 9.6 to make working solutions. The peptides were applied as lines on a nylon membrane (Pall, Portsmouth, United Kingdom), after which the membrane was treated with casein to block unoccupied binding sites. The membrane was subsequently cut into strips perpendicular to the direction of the peptide lines. Each strip was then incubated with a serum sample diluted 1 to 100, obtained from an HCV-infected individual. Antibody binding was detected by incubating the strips with goat anti-human immunoglobulin antibodies conjugated to the enzyme alkaline phosphatase. After removing unbound conjugate by washing, a substrate solution containing 5-bromo-4-chloro-3-indolylphosphate and nitro blue tetrazolium was added. Positive reactions are visible as colored lines corresponding to the positions of the peptides which are specifically recognized. The reaction patterns of thirty-six different sera are tabulated in Table 1. The results shown in Table 1 are further summarized in Table 2.
B. Use of peptides in an enzyme-linked immunosorbent assay (ELISA). Peptide stock solutions were diluted in sodium carbonate buffer, pH 9.6 and used to coat microtiter plates at a peptide concentration of 2 micrograms per milliliter. A mixture consisting of peptides II, III, V, IX, and XVIII was also used to coat plates. Following coating, the plates were blocked with casein. Fifteen HCV-antibody-positive sera and control sera from seven uninfected blood donors were diluted 1 to 20 and incubated in wells of the peptide-coated plates. Antibody binding was detected by incubating the plates with goat anti-human immunoglobulin antibodies conjugated to the enzyme horseradish peroxidase. Following removal of unbound conjugate by washing, a solution containing H₂O₂ and 3,3',5,5'-tetramethylbenzidine was added. Reactions were stopped after a suitable interval by addition of sulfuric acid. Positive reactions gave rise to a yellow color which was quantified using a conventional microtiter plate reader. The results of these determinations are tabulated in Table 3. To correct for any aspecific binding which could be attributable to the physical or chemical properties of the peptides themselves, a cut-off value was determined for each peptide individually. This cut-off absorbance value was calculated as the average optical density of the negative samples plus 0.200. Samples giving absorbance values higher than the cut-off values are considered positive. The results for the fifteen positive serum samples are further summarized in Table 4. While it is evident that some of the peptides are recognized by a large percentage of sera from HCV-infected individuals, it is also clear that no single peptide is recognized by all sera. In contrast, the peptide mixture was recognized by all fifteen sera and, for six of the fifteen sera, the optical densities obtained were equal to or higher than those obtained for any of the peptides individually. These results serve to illustrate the advantages of using mixtures of peptides for the detection of anti-HCV antibodies.
C. Binding of antibodies in sera from HCV-infected patients to various individual peptides and peptide mixtures in an ELISA. Five peptides were used individually and in seven different combinations to coat microtiter plates. The plates were subsequently incubated with dilutions of fifteen HCV antibody-positive sera in order to evaluate the relative merits of using mixtures as compared to individual peptides for antibody detection. The mixtures used and the results obtained are shown in Figure 2. In general, the mixtures functioned better than individual peptides. This was particularly evident for mixture 12 (peptides I, III, V, IX, and XVIII) which was recognized by all twelve of the sera tested. These results underscore the advantages of using mixtures of peptides in diagnostic tests for the detection of antibodies to HCV.
D. Use of a mixture of peptides in an ELISA assay for the detection of anti-HCV antibodies. A mixture of peptides II, III, V, IX, and XVIII was prepared and used to coat microtiter plates according to the same procedure used to test the individual peptides. A total of forty-nine sera were tested from patients with clinically diagnosed but undifferentiated chronic non A non B hepatitis as well as forty-nine sera from healthy blood donors. Detection of antibody binding was accomplished using goat anti-human immunoglobulin antibodies conjugated to horseradish peroxidase. The resulting optical density values are given in Table 5. These results indicate that the mixture of peptides is not recognized by antibodies in sera from healthy donors (0/49 reactives) but is recognized by a large proportion (41/49, or 84%) of the sera from patients with chronic NANBH. These results demonstrate that the peptides described can be used effectively as mixtures for the diagnosis of HCV infection.
E. Detection of anti-HCV antibodies in sera from patients with acute NANB infection using individual peptides bound to nylon membranes and a mixture of peptides in an ELISA assay, and comparison with a commercially available kit. Peptides were applied to nylon membranes or mixed and used to coat microtiter plates as previously described. The peptide mixture consisted of peptides II, III, V, IX, and XVIII. Sera obtained from twenty-nine patients with acute non-A, non-B hepatitis were then tested for the presence of antibodies to hepatitis C virus. These same sera were also evaluated using a commercially available kit (Ortho, Emeryville, CA, USA).
The results of this comparative study are given in Table 6. In order to be able to compare the peptide-based ELISA with the commercially available kit, the results for both tests are also expressed as signal to noise ratios (S/N) which were calculated by dividing the measured optical density obtained for each sample by the cut-off value. A signal-to-noise ratio greater or equal to 1.0 is taken to represent a positive reaction. For the commercially available kit, the cut-off value was calculated according to the manufacturer's instructions. The cut-off value for the peptide-based ELISA was calculated as the average optical density of five negative samples plus 0.200.
The scale used to evaluate antibody recognition of nylon-bound peptides was the same as that given in Table 1. Of the twenty-nine samples tested, twenty-five (86%) were positive in the peptide-based ELISA and recognized one or more nylon-bound peptides. In contrast, only fourteen of the twenty-nine sera scored positive in the commercially available ELISA. These results serve to illustrate the advantages of using peptide mixtures for the detection of anti-HIV antibodies as well as the need to include in the mixtures peptides which contain amino acid sequences derived from different regions of the HCV polyprotein.

Summary of antibody binding to nylon-bound HCV peptides by sera from infected patients.
Peptide	No. reactive sera	% reactive sera
I	13/35	37
II	22/35	63
III	27/35	77
IV	24/35	69
V	14/35	40
VI	11/35	31
VII	11/35	31
VIII	19/36	53
IX	9/36	25
X	17/36	47
XI	15/36	42
XII	1/36	3
XIII	13/36	36
XIV	7/36	19
XV	9/36	25
XVI	20/36	56
XVII	14/36	39
XVIII	14/36	39
XIX	8/36	22

Summary of antibody-binding to individual peptides in an ELISA assay.
Peptide	No. reactive sera	% reactive sera
I	13	87
II	13	87
III	14	93
IV	10	67
V	10	67
VI	7	47
VII	8	53
VIII	13	87
IX	12	80
X	13	87
XI	13	87
XII	1	7
XIII	7	47
XIV	8	53
XV	2	13
XVI	5	33
XVII	4	27
XVIII	10	67
XIX	6	40

Claims

A peptide composition comprising at least one peptide selected from :

wherein Y is H or a linker arm by which the peptide can be attached to a carrier or solid phase comprising at least one amino acid and as many as 60, most frequently 1 to 10 amino acids, such as cysteine, lysine, tyrosine, glutamic acid or aspartic acid, or chemical groups such as biotin or thioglycolic acid, Y can be modified by for instance N-terminal acetylation; Z is a bond or a linker arm by which the peptide can be attached to a carrier or solid phase comprising at least one amino acid and as many as 60 amino acids, most frequently 1 to 10 amino acids, such as cysteine, lysine, tyrosine, glutamic acid or aspartic acid, or chemical groups such as biotin or thioglycolic acid; and X is NH₂, OH or a linkage involving either of these two groups and provided that when Y or Z-X are (an) amino acid(s), they are different from any naturally occurring HCV flanking regions.
A peptide composition according to claim 1, further characterized in that said peptides are coupled N-terminally, C-terminally or internally to a carrier molecule for the purpose of raising antibodies or facilitating the adsorption of said peptides to a solid phase.
A peptide composition according to claims 1 or 2, further characterized in that said peptides contain a detectable label.
Use of a peptide composition according to any of claims 1 tot 3, for the incorporation into an immunoassay for detecting the presence of antibodies to Hepatitis C virus present in a body fluid.
A method for the in vitro detection of antibodies to hepatitis C virus present in a body fluid such as serum or plasma, comprising at least the steps of :

(a) contacting body fluid of a person to be diagnosed with a peptide composition according to any of claims 1 to 3, and,

(b) detecting the immunological complex formed between said antibodies and the peptide(s) used.
A kit for the detection of anti-hepatitis C virus antibodies in a body fluid, comprising at least the following components :

a peptide composition according to any of claims 1 to 3,

a means for detecting an immunological complex formed between said peptides and said antibodies.
A method according to claim 5, further characterized in that said peptides are applied as lines on a nylon membrane, and with said nylon membrane being preferably cut into strips perpendicular to the direction of the peptide lines, thus allowing each strip to be incubated with an appropriately diluted serum sample from an individual.
A kit according to claim 6, further characterized in that said peptides are applied as lines on a nylon membrane, and with said nylon membrane being preferably cut into strips perpendicular to the direction of the peptide lines, thus allowing each strip to be incubated with an appropriately diluted serum sample from an individual.
A kit according to any of claims 6 or 8, further characterized in that said peptides, seperately or in combination, are used to coat the wells of microtiter plates.
Use of a peptide composition according to any of claims 1 to 3, for incorporation into a vaccine composition against HCV.
Peptide composition according to any one of claims 1 to 3, for raising antibodies against HCV.
Peptide composition according to any one of claims 1 to 3, wherein said peptides are such as obtained by cyclizing any of the peptides of claim 1, or by coupling together two peptides of claim 1.
Peptide composition according to any one of claims 1 to 3, wherein said peptides are such as obtained by synthetizing the peptides of claim 1 directly on an oligolysine core in which both the alpha as well as the epsilon-amino groups of lysines are used as growth points for the peptides.
Process for preparing a peptide composition comprising at least one peptide selected from:

wherein Y is H or a linker arm by which the peptide can be attached to a carrier or solid phase comprising at least one amino acid and as many as 60, most frequently 1 to 10 amino acids, such as cysteine, lysine, tyrosine, glutamic acid or aspartic acid, or chemical groups such as biotin or thioglycolic acid, Y can be modified by for instance N-terminal acetylation; Z is a bond or a linker arm by which the peptide can be attached to a carrier or solid phase comprising at least one amino acid and as many as 60 amino acids, most frequently 1 to 10 amino acids, such as cysteine, lysine, tyrosine, glutamic acid or aspartic acid, or chemical groups such as biotin or thioglycolic acid; and X is NH₂, OH or a linkage involving either of these two groups and provided that when Y or Z-X are (an) amino acid(s), they are different from any naturally occurring HCV flanking regions, with said peptides being synthesized in solution or on a solid support employing t-butyloxycarbonyl- or 9-fluorenylmethoxy-carbonyl-protected activated amino acids, and with said peptides being mixed in case different peptides are comprised in said composition.
Process according to claim 14, further characterized in that said peptides are coupled N-terminally, C-terminally or internally to a carrier molecule for the purpose of raising antibodies or facilitating the adsorption of said peptides to a solid phase.
Process according to any of claims 14 to 15, characterized in that said peptides contain a detectable label added to said peptide.
Process for the preparation of a kit for the detection of anti-hepatitis C virus antibodies in a body fluid, comprising gathering at least the following components :

a peptide composition according to claim 1,

a means for detecting an immunological complex formed between said peptides and said antibodies.
Process for the preparation of a kit according to claim 17, further characterized in that said peptides are applied as lines on a nylon membrane, and with said nylon membrane being preferably cut into stripts perpendicular to the direction of the peptide lines, thus allowing each strip to be incubated with an appropriately diluted serum sample from an individual.
Process for the preparation of a kit according to claim 17 of 18, further characterized in that said peptides, seperately or in combination, are used to coat the wells of microtiter plates.
Process for the preparation of a peptide composition according to any one of claims 14 to 16, for incorporation into a vaccine composition against HCV.
Process for the preparation of a peptide composition according to any one of claims 14 to 16, for raising antibodies against HCV.
Process for the preparation of a peptide composition to any one of claims 14 to 16, wherein said peptides are such as obtained by cyclizing any of the peptides of claim 1, or by coupling together two peptides of claim 1.
Process for the preparation of a peptide composition according to any one of claims 14 to 16, wherein said peptides are such as obtained by synthetizing the peptides of claim 1 directly on an oligo-lysine core in which both the alpha as well as the epsilon-amino groups of lysines are used as growth points for the peptides.